EP2646229B1 - Revêtement à plasma atmosphérique pour dispositifs ophtalmologiques - Google Patents

Revêtement à plasma atmosphérique pour dispositifs ophtalmologiques Download PDF

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Publication number
EP2646229B1
EP2646229B1 EP11797068.1A EP11797068A EP2646229B1 EP 2646229 B1 EP2646229 B1 EP 2646229B1 EP 11797068 A EP11797068 A EP 11797068A EP 2646229 B1 EP2646229 B1 EP 2646229B1
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Prior art keywords
plasma
pyrrolidone
carbon atoms
methylene
silicone hydrogel
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German (de)
English (en)
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EP2646229A1 (fr
Inventor
Yongxing Qiu
John Dallas Pruitt
Chandana Kolluru
Maria A. Dunkle
Yasuo Matsuzawa
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Novartis AG
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Novartis AG
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00—Producing optical elements, e.g. lenses or prisms
    • B29D11/00009—Production of simple or compound lenses
    • B29D11/00038—Production of contact lenses
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D11/00—Producing optical elements, e.g. lenses or prisms
    • B29D11/00865—Applying coatings; tinting; colouring

Definitions

  • the present invention relates generally to the field of ophthalmic devices, and more particularly to surface coating of ophthalmic devices to control the increase or decrease of wettability.
  • silicone hydrogel contact lenses it is desirable that the surfaces of silicone hydrogel contact lenses are readily wettable by an aqueous liquid, such as tear fluid, and are capable of retaining an aqueous fluid layer which is beneficial for the comfort of the wearer.
  • soft silicone hydrogel contact lenses typically have hydrophobic surfaces or at least some hydrophobic surfaces areas and are required to be subjected to surface treatment to render the surfaces wettable, hydrophilic, and less susceptible to depositions of proteins and/or lipids from the ocular environment.
  • the effect of surface treatment should be durable and the modified surfaces should exhibit thermal, oxidative and hydrolytic stability as well as resistance to formation of deposits from tear components and delamination caused by mechanical stress.
  • plasma denotes an ionized gas (e.g., created by electric glow discharge which may be composed of electrons, ions of either polarity, gas atoms and molecules in the ground or any higher state of any form of excitation, as well as of photons).
  • This ionized gas is often called "low temperature plasma”.
  • the known plasma treatment under low pressure includes plasma deposition, plasma-induced polymerization, plasma grafting, plasma oxidation, and the likes.
  • WO 2000/71613 is related to an optically clear, hydrophilic coating upon the surface of a silicone medical device, which is obtained by sequentially subjecting the surface of the lens to plasma polymerization in a hydrocarbon-containing atmosphere and then covalently attaching a preformed hydrophilic polymer to the surface of the carbon coating.
  • the plasma polymerization used in the carbon coating is a "standard plasma oxidation and deposition process (also referred to as 'electrical glow discharge process')" at low pressure conducted on contact lenses in their unhydrated state.
  • Plasma treatment under low pressure haven been used in commercial products, for example, such as, Focus NIGHT & DAY TM and O20PTIX TM (CIBA VISION), and PUREVISIONTM (Bausch & Lomb).
  • Advantages of a plasma coating such as, e.g., those may be found with Focus NIGHT & DAYTM, are its durability, relatively high hydrophilicity/wettability), and low susceptibility to lipid and protein deposition and adsorption.
  • plasma treatment under low pressure of silicone hydrogel contact lenses may not be cost effective, because the preformed contact lenses must typically be dried before plasma treatment and because of relative high capital investment associated with plasma treatment equipment.
  • the present invention is primarily directed to improved coating processes and coatings for ophthalmic devices and other objects without pre-drying them.
  • the present invention relates to a method for producing ready-to-use silicone hydrogel contact lenses each having a durable plasma hydrophilic coating.
  • the method comprises the steps of: (a) generating an atmospheric plasma flow from a working gas by atmospheric pressure discharges at a surrounding atmospheric pressure , wherein the working gas comprises at least one organic compound selected from the group consisting of a C 1 -C 12 alkane, an oxaalkane having up to 12 carbon atoms, a C 2 -C 12 alkene, an oxaalkene having up to 12 carbon atoms, a C 2 -C 12 alkyne, a C 1 -C 12 alkanol, a cycloalkanol having up to 12 carbon atoms, an oxaalkyne having up to 12 carbon atoms, a mono- cyclooxaalkane having up to 12 carbon atoms, a bi- cyclooxaalkane having up to 12 carbon atoms, a tricycl
  • ophthalmic lens refers to an intraocular lens, a contact lens (hard or soft), or a corneal onlay.
  • Contact Lens refers to a structure that can be placed on or within a wearer's eye. A contact lens can correct, improve, or alter a user's eyesight, but that need not be the case.
  • a contact lens can be of any appropriate material known in the art or later developed, and can be a soft lens, a hard lens, or a hybrid lens.
  • silicone hydrogel contact lens refers to a contact lens comprising a silicone hydrogel material.
  • hydrogel or “hydrogel material” refers to a crosslinked polymeric material which is not water-soluble and can contains at least 10% by weight of water within its polymer matrix when fully hydrated.
  • non-silicone hydrogel refers to a hydrogel that is theoretically free of silicon.
  • silicone hydrogel refers to a hydrogel containing silicone.
  • a silicone hydrogel typically is obtained by copolymerization of a polymerizable composition comprising at least one silicone-containing vinylic monomer or at least one silicone-containing vinylic macromer or at least one silicone-containing prepolymer having ethylenically unsaturated groups.
  • vinylenically unsaturated group refers to a compound that has one sole ethylenically unsaturated group and can be polymerized actinically or thermally.
  • hydrophilic vinylic monomer refers to a vinylic monomer which as a homopolymer typically yields a polymer that is water-soluble or can absorb at least 10 percent by weight water.
  • hydrophobic vinylic monomer refers to a vinylic monomer which as a homopolymer typically yields a polymer that is insoluble in water and can absorb less than 10 percent by weight water.
  • the term "macromer” or “prepolymer” refers to a medium and high molecular weight compound or polymer that contains two or more ethylenically unsaturated groups.
  • Medium and high molecular weight typically means average molecular weights greater than 700 Daltons.
  • crosslinker refers to a compound having at least two ethylenically unsaturated groups.
  • a “crosslinking agent” refers to a crosslinker having a molecular weight of about 700 Daltons or less.
  • water contact angle refers to an average water contact angle (i.e., contact angles measured by Sessile Drop method), which is obtained by averaging measurements of contact angles.
  • polymer means a material formed by polymerizing/crosslinking one or more monomers or macromers or prepolymers.
  • molecular weight of a polymeric material refers to the weight-average molecular weight unless otherwise specifically noted or unless testing conditions indicate otherwise.
  • fluid indicates that a material is capable of flowing like a liquid.
  • the present invention is an atmospheric plasma coating ("APC”), or APC treatment deposition process and coating chemistry, for achieving "wettable" coatings on a substrate.
  • APC atmospheric plasma coating
  • APC treatment deposition process and coating chemistry for achieving "wettable” coatings on a substrate.
  • Atmospheric plasma is typically understood to be plasma sustained at a surrounding atmospheric pressure and can be produced by atmospheric pressure discharges.
  • Example atmospheric pressure discharges include arc discharge, which is a high power thermal discharge of very high temperature (i.e., about 10,000K).
  • Arc discharge can be generated using various power supplies and is commonly used in metallurgical processes. For example, arc discharge is used to melt rocks containing Al 2 O 3 to produce aluminum.
  • Corona discharge is another atmospheric pressure discharge that is a non-thermal discharge generated by the application of high voltage to sharp electrode tips. Corona discharge is commonly used in ozone generators and particle precipitators.
  • a further atmospheric pressure discharge is a dielectric barrier discharge (DBD), which is a non-thermal discharge generated by the application of high voltages across small gaps wherein a non-conducting coating prevents the transition of the plasma discharge into an arc.
  • DBD dielectric barrier discharge
  • the example APC process utilizes a plasma treatment system (e.g., PT-2000 and PT-2000P manufactured by Tri-Star Technologies) including a plasma generator and a plasma nozzle.
  • a plasma treatment system e.g., PT-2000 and PT-2000P manufactured by Tri-Star Technologies
  • an example plasma treatment system 10 includes a system control panel 12, a plasma generator 14, a plasma electrode 16, a plasma nozzle 18 and a handle 20.
  • the plasma generator 14 includes a power supply, gas flow controller 22 and a power amplifier 24.
  • the plasma generator 14 feeds electrical signals with specific amplitude, frequency and form factor to the primary winding of high voltage transformer.
  • the generator 14 can produce a continuous stream of plasma. Alternatively, appropriately shaped electrical pulses with a defined amplitude and frequency produced by the transformer secondary winding are applied to the plasma electrode 16.
  • An example power supply subassembly includes an AC inlet connector, an AC filter, a pre-defined ampere fuse and a DC power supply that is used for the gas controller.
  • the system control panel 12 allows an operator to change system parameters, such as carrier gas (e.g., inert gas) flow, plasma intensity and exposure time, and monitor system errors.
  • the example system control panel 12 includes a timer (not shown) that allows a user to set a precise exposure time.
  • plasma jets exit the nozzle 18 and reach a substrate to then spread over the substrate surface.
  • the plasma jets preferably exit the nozzle 18 at atmospheric pressure. If the substrate is two-sided, a user can turn the substrate over with tweezers and coat the opposing surface with the plasma jet.
  • the example plasma treatment system 10 can alternatively generate a uniform plasma cloud that completely surrounds, or spreads over, the boundary layer of a substrate surface.
  • the example plasma cloud can occupy a finite volume of space filled with a gas at a defined temperature (e.g., about room temperature).
  • the plasma typically exists in the surface boundary layer in the vicinity of the nozzle 18 and abruptly decays due to contact with air.
  • a carrier gas e.g., inert gas: helium, argon or xenon
  • the charged particle can either ionize to produce another charged particle (i.e., electron and ion) or move apart from the atom.
  • a relative concentration of ions and electrons in the plasma can be on the order of about 1 ppm. Therefore, a very minute percentage of the carrier gas can be involved in the treatment process.
  • a small amount of reagent gases and/or gas mixtures e.g., air, acetylene, oxygen etc.
  • FIG. 2 shows an alternate system for introducing such a gaseous mixture into the plasma flow.
  • an example system includes a plasma electrode 26 connected to a nozzle 32 through an adaptor 28.
  • an additional reagent gas mixture line 34 introduces reagent gas to the plasma flow within the nozzle 32 through a connector 30.
  • the reagent gas mixture line 34 preferably provides a reagent gas from a flowmeter separate from the system.
  • the plasma jet 36 exiting the nozzle 32 additionally includes a carrier gas.
  • An example plasma jet 36 exiting the nozzle 32 can include a reagent gas mixture during a coating procedure. When the jet 34 contacts a substrate surface, the gaseous reagent and plasma spreads over a thin boundary layer.
  • the APC plasma treatment or coating process can alternatively occur within a chamber 38 operable between two insulated metal electrodes 40, 42.
  • the chamber 38 can be defined by a shell or housing.
  • An example chamber 38 can include a gas-in conduit (or valve) 49 and a gas-out conduit (or valve) 46 to regulate flow, pressure and concentration of plasma gas within the chamber.
  • the gas-in conduit 49 can be adapted to connect, and receive plasma from, to the plasma nozzle of the plasma system ( Figures 1 and 2 ).
  • the gas-in conduit 49 can be adapted to connect to, and receive plasma from, a separate plasma delivery source (e,g., plasma generator).
  • the gas-out conduit 46 releases plasma from the chamber 38.
  • the chamber 38 housing can have a shape resembling a cylinder with open ends and it can also have other shapes. The open ends can be sealed with the insulated metal electrodes 40, 42.
  • the example chamber 38 housing is constructed of an impermeable material (e.g., glass or plastic).
  • the substrate to-be-coated can be secured within the chamber 38 such that plasma flowing through the chamber spreads across all surfaces of the substrate.
  • the volume of the example chamber 38 can be varied based upon the size of the substrate to be treated or coated, or based on the power of the plasma controller.
  • the example APC process can be carried out using a consistent plasma cloud that can be generated by a nozzle or filling a chamber by incorporating reagent gas mixture and/or hydrophilic vinylic monomer(s) (e.g., DMA, NVP, HEMA, HEA, and those described below or known to a person skilled in the art).
  • the APC process can be effected by using a pulsed mode of plasma coating and by incorporating hydrophilic vinylic monomer(s) (e.g., DMA, NVP, HEMA, HEA, and those described below or known to a person skilled in the art).
  • the pulsed plasma mode the plasma is pulsed according to preset intervals manipulated by the power source.
  • Example pulse intervals used can include a range of between about 0.1 millisecond and 3 milliseconds, and more preferably about 1 millisecond.
  • An example substrate to be coated according to the system and method of the present invention includes contact lenses, intraocular lenses, and more specifically silicon-hydrogel (SiHy) contact lenses.
  • any silicone hydrogel contact lenses can be coated according to a method of the invention.
  • a person skilled in the art knows very well how to make contact lenses.
  • contact lenses can be produced in a conventional "spin-casting mold," as described for example in U.S. Patent No. 3,408,429 , or by the full cast-molding process in a static form, as described in U.S. Patent Nos. 4,347,198 ; 5,508,317 ; 5,583,463 ; 5,789,464 ; and 5,849,810 .
  • the first and second molding surface of a mold are pressed against each other to form a circumferential contact line which defines the edge of a result contact lens. Because the close contact of the molding surfaces can damage the optical quality of the molding surfaces, the mold cannot be reused. In contrast, in a Lightstream Technology TM , the edge of a resultant contact lens is not defined by the contact of the molding surfaces of a mold, but instead by a spatial limitation of radiation. Without any contact between the molding surfaces of a mold, the mold can be used repeatedly to produce high quality contact lenses with high reproducibility.
  • a "spatial limitation of actinic radiation” refers to an act or process in which energy radiation in the form of rays is directed by, for example, a mask or screen or combinations thereof, to impinge, in a spatially restricted manner, onto an area having a well defined peripheral boundary.
  • a spatial limitation of UV radiation is obtained by using a mask or screen having a radiation (e.g.,UV) permeable region, a radiation (e.g., UV) impermeable region surrounding the radiation-permeable region, and a projection contour which is the boundary between the radiation-impermeable and radiation-permeable regions, as schematically illustrated in the drawings of U.S. Patent Nos. 6,800,225 ( Figs. 1-11 ), and 6,627,124 ( Figs.
  • the mask or screen allows to spatially projects a beam of radiation (e.g., UV radiation) having a cross-sectional profile defined by the projection contour of the mask or screen.
  • the projected beam of radiation e.g., UV radiation
  • limits radiation e.g., UV radiation
  • the resultant contact lens comprises an anterior surface defined by the first molding surface, an opposite posterior surface defined by the second molding surface, and a lens edge defined by the sectional profile of the projected UV beam (i.e., a spatial limitation of radiation).
  • the radiation used for the crosslinking is a radiation energy, especially UV radiation, gamma radiation, electron radiation or thermal radiation, the radiation energy preferably being in the form of a substantially parallel beam in order on the one hand to achieve good restriction and on the other hand efficient use of the energy.
  • a mold for cast molding
  • a mold generally comprises at least two mold sections (or portions) or mold halves, i.e. first and second mold halves.
  • the first mold half defines a first molding (or optical) surface and the second mold half defines a second molding (or optical) surface.
  • the first and second mold halves are configured to receive each other such that a lens forming cavity is formed between the first molding surface and the second molding surface.
  • the molding surface of a mold half is the cavity-forming surface of the mold and in direct contact with lens-forming material.
  • Methods of manufacturing mold sections for cast-molding a contact lens are generally well known to those of ordinary skill in the art.
  • the process of the present invention is not limited to any particular method of forming a mold. In fact, any method of forming a mold can be used in the present invention.
  • the first and second mold halves can be formed through various techniques, such as injection molding or lathing. Examples of suitable processes for forming the mold halves are disclosed in U.S. Patent Nos. 4,444,711 to Schad ; 4,460,534 to Boehm et al. ; 5,843,346 to Morrill ; and 5,894,002 to Boneberger et al. .
  • Virtually all materials known in the art for making molds can be used to make molds for making contact lenses.
  • polymeric materials such as polyethylene, polypropylene, polystyrene, PMMA, Topas® COC grade 8007-S10 (clear amorphous copolymer of ethylene and norbornene, from Ticona GmbH of Frankfurt, Germany and Summit, New Jersey), or the like can be used.
  • Other materials that allow UV light transmission could be used, such as quartz glass and sapphire.
  • reusable molds are used and the silicone-hydrogel lens-forming composition is cured actinically under a spatial limitation of actinic radiation to form a SiHy contact lens.
  • preferred reusable molds are those disclosed in U.S. patent application Nos. 08/274,942 filed July 14, 1994 , 10/732,566 filed December 10, 2003 , 10/721,913 filed November 25, 2003 , and U.S. Patent No. 6,627,124 .
  • Reusable molds can be made of quartz, glass, sapphire, CaF2, a cyclic olefin copolymer (such as for example, Topas® COC grade 8007-S10 (clear amorphous copolymer of ethylene and norbornene) from Ticona GmbH of Frankfurt, Germany and Summit, New Jersey, Zeonex® and Zeonor® from Zeon Chemicals LP, Louisville, KY), polymethylmethacrylate (PMMA), polyoxymethylene from DuPont (Delrin), Ultem® (polyetherimide) from G.E. Plastics, PrimoSpire®, etc.
  • a cyclic olefin copolymer such as for example, Topas® COC grade 8007-S10 (clear amorphous copolymer of ethylene and norbornene) from Ticona GmbH of Frankfurt, Germany and Summit, New Jersey, Zeonex® and Zeonor® from Zeon Chemicals LP, Louisville, KY
  • PMMA polymethylme
  • a lens formulation typically is dispensed into molds and cured (i.e., polymerized and/or crosslinked) in molds for making contact lenses.
  • a silicone hydrogel (SiHy) contact lens formulation for cast-molding or spin-cast molding of contact lenses generally comprises at least one components selected from the group consisting of a silicone-containing vinylic monomer, a silicone-containing vinylic macromer, a silicone-containing prepolymer, a hydrophilic vinylic monomer, a hydrophobic vinylic monomer, a crosslinking agent (a compound having a molecular weight of about 700 Daltons or less and containing at least two ethylenically unsaturated groups), a free-radical initiator (photoinitiator or thermal initiator), a hydrophilic vinylic macromer/prepolymer, and combination thereof, as well known to a person skilled in the art.
  • a SiHy contact lens formulation can also comprise other necessary components known to a person skilled in the art, such as, for example, a UV-absorbing agent, a visibility tinting agent (e.g., dyes, pigments, or mixtures thereof), antimicrobial agents (e.g., preferably silver nanoparticles), a bioactive agent, leachable lubricants, leachable tear-stabilizing agents, and mixtures thereof, as known to a person skilled in the art.
  • a UV-absorbing agent e.g., a visibility tinting agent (e.g., dyes, pigments, or mixtures thereof), antimicrobial agents (e.g., preferably silver nanoparticles), a bioactive agent, leachable lubricants, leachable tear-stabilizing agents, and mixtures thereof, as known to a person skilled in the art.
  • a visibility tinting agent e.g., dyes, pigments, or mixtures thereof
  • antimicrobial agents e.g., preferably silver nanoparticles
  • a SiHy lens formulation can be a solution or a melt at a temperature from about 20°C to about 85°C.
  • a polymerizable composition is a solution of all desirable components in a suitable solvent, or a mixture of suitable solvents.
  • a SiHy lens formulation can be prepared by dissolving all of the desirable components in any suitable solvent, such as, water, a mixture of water and one or more organic solvents miscible with water, an organic solvent, or a mixture of one or more organic solvents, as known to a person skilled in the art.
  • suitable solvent such as, water, a mixture of water and one or more organic solvents miscible with water, an organic solvent, or a mixture of one or more organic solvents, as known to a person skilled in the art.
  • Example of preferred organic solvents includes without limitation, tetrahydrofuran, tripropylene glycol methyl ether, dipropylene glycol methyl ether, ethylene glycol n-butyl ether, ketones (e.g., acetone, methyl ethyl ketone, etc.), diethylene glycol n-butyl ether, diethylene glycol methyl ether, ethylene glycol phenyl ether, propylene glycol methyl ether, propylene glycol methyl ether acetate, dipropylene glycol methyl ether acetate, propylene glycol n-propyl ether, dipropylene glycol n-propyl ether, tripropylene glycol n-butyl ether, propylene glycol n-butyl ether, dipropylene glycol n-butyl ether, tripropylene glycol n-butyl ether, propylene glycol n-butyl ether, diprop
  • Molded silicone hydrogel contact lenses then can be subjected to extraction with an extraction solvent to remove unpolymerized components from the molded lenses and to hydration process, as known by a person skilled in the art.
  • Numerous SiHy lens formulations have been described in numerous patents and patent applications published by the filing date of this application. All of them can be used in a method of the invention.
  • a SiHy lens formulation for making commercial SiHy lenses such as, lotrafilcon A, lotrafilcon B, balafilcon A, galyfilcon A, senofilcon A, narafilcon A, narafilcon B, comfilcon A, enfilcon A, asmofilcon A, filcon II 3, can also be used in a method of the invention.
  • wet used in this application in reference to a contact lens (including a silicone hydrogel contact lens) means that the contact lens is in a hydrated state (by water) and still has a water content that is at least about 50%, preferably at least about 65%, more preferably at least about 80%, even more preferably at least about 90% (by weight) of the equilibrium water content (i.e., the value of the water content when the contact lens is fully hydrated).
  • blot-dried used in this application in reference to a contact lens (including a silicone hydrogel contact lens) means that water on the surface of a contact lens is removed with a lint-free clean cloth or a clean paper tissue or a stream of clean air.
  • durable used in this application in reference with a coating on a contact lens (including a silicone hydrogel contact lens) means that the hydrophilicity/wettability of the coating on the contact lens is not significantly decreased after the contact lens is autoclaved in a phosphate buffered saline at about 121°C for one autoclave cycle (i.e., one thirty-minutes cycle), preferably for two autoclave cycle (i.e., two thirty-minutes cycles), as characterized by no significant increase in water contact angle (i.e., more than 30% increase) and/or by having a water break up time (WBUT, determined as described below) of at least about 5 seconds.
  • one autoclave cycle i.e., one thirty-minutes cycle
  • two autoclave cycle i.e., two thirty-minutes cycles
  • WBUT water break up time
  • a coating on a contact lens especially a silicone hydrogel contact lens
  • a silicone hydrogel contact lens it is important for a coating on a contact lens, especially a silicone hydrogel contact lens, to survive at least one autoclave cycle, because ready-to-use contact lenses are required to be sterilized, i.e., autoclaved at about 115-125°C for at least about twenty minutes. It is believed that silicone components in a silicone hydrogel contact lens tend to migrate to the lens surface when being exposed to air or during autoclave. Any coating on a silicone hydrogel contact lens cannot survive at least one autoclave cycle is not durable but transient.
  • an atmospheric plasma coating process of the invention can reduce the time, energy and cost required to dry the silicone hydrogel contact lenses.
  • silicone hydrogel contact lenses with plasma coating obtained according to an atmospheric plasma coating method of the invention are sterilized by autoclaving the plasma-coated silicone hydrogel contact lenses each immersed in a packaging solution (i.e., a buffered aqueous solution) in a sealed lens package at a temperature of from about 115°C to about 125°C for approximately 20-90 minutes.
  • a packaging solution i.e., a buffered aqueous solution
  • the packaging solution is a buffered aqueous solution which is ophthalmically safe after autoclave.
  • Lens packages are well known to a person skilled in the art for autoclaving and storing a soft contact lens. Any lens packages can be used in the invention.
  • a lens package is a blister package which comprises a base and a cover, wherein the cover is detachably sealed to the base, wherein the base includes a cavity for receiving a sterile packaging solution and the contact lens.
  • Lenses are packaged in individual packages, sealed, and sterilized (e.g., by autoclave at about 120°C or higher for at least 30 minutes) prior to dispensing to users.
  • autoclave at about 120°C or higher for at least 30 minutes
  • a person skilled in the art will understand well how to seal and sterilize lens packages.
  • a packaging solution contains at least one buffering agent and one or more other ingredients known to a person skilled in the art.
  • other ingredients include without limitation, tonicity agents, surfactants, antibacterial agents, preservatives, and lubricants (or water-soluble viscosity builders) (e.g., cellulose derivatives, polyvinyl alcohol, polyvinylpyrrolidone).
  • the packaging solution contains a buffering agent in an amount sufficient to maintain a pH of the packaging solution in the desired range, for example, preferably in a physiologically acceptable range of about 6 to about 8.5.
  • a buffering agent in an amount sufficient to maintain a pH of the packaging solution in the desired range, for example, preferably in a physiologically acceptable range of about 6 to about 8.5.
  • Any known, physiologically compatible buffering agents can be used.
  • Suitable buffering agents as a constituent of the contact lens care composition according to the invention are known to the person skilled in the art. Examples are boric acid, borates, e.g. sodium borate, citric acid, citrates, e.g. potassium citrate, bicarbonates, e.g.
  • TRIS (2-amino-2-hydroxymethyl-1,3-propanediol), Bis-Tris (Bis-(2-hydroxyethyl)-imino-tris-(hydroxymethyl)-methane), bis-aminopolyols, triethanolamine, ACES (N-(2-hydroxyethyl)-2-aminoethanesulfonic acid), BES (N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid), HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid), MES (2-(N-morpholino)ethanesulfonic acid), MOPS (3-[N-morpholino]-propanesulfonic acid), PIPES (piperazine-N,N'-bis(2-ethanesulfonic acid), TES (N-[Tris(hydroxymethyl)methyl]-2-aminoethanesulfonic acid), salt
  • each buffer agent in a packaging solution is preferably from 0.001% to 2%, preferably from 0.01% to 1%; most preferably from about 0.05% to about 0.30% by weight.
  • the packaging solution has a tonicity of from about 200 to about 450 milliosmol (mOsm), preferably from about 250 to about 350 mOsm.
  • the tonicity of a packaging solution can be adjusted by adding organic or inorganic substances which affect the tonicity.
  • Suitable occularly acceptable tonicity agents include, but are not limited to sodium chloride, potassium chloride, glycerol, propylene glycol, polyols, mannitols, sorbitol, xylitol and mixtures thereof.
  • a packaging solution of the invention has a viscosity of from about 1 centipoise to about 20 centipoises, preferably from about 1.5 centipoises to about 10 centipoises, more preferably from about 2 centipoises to about 5 centipoises, at 25°C.
  • the packaging solution comprises preferably from about 0.01% to about 2%, more preferably from about 0.05% to about 1.5%, even more preferably from about 0.1% to about 1%, most preferably from about 0.2% to about 0.5%, by weight of a water-soluble and thermally-crosslinkable hydrophilic polymeric material of the invention.
  • a packaging solution of the invention can contain a viscosity-enhancing polymer.
  • the viscosity-enhancing polymer preferably is nonionic. Increasing the solution viscosity provides a film on the lens which may facilitate comfortable wearing of the contact lens.
  • the viscosity-enhancing component may also act to cushion the impact on the eye surface during insertion and serves also to alleviate eye irritation.
  • Preferred viscosity-enhancing polymers include, but are not limited to, water soluble cellulose ethers (e.g., methyl cellulose (MC), ethyl cellulose, hydroxymethylcellulose, hydroxyethyl cellulose (HEC), hydroxypropylcellulose (HPC), hydroxypropylmethyl cellulose (HPMC), or a mixture thereof), water-soluble polyvinylalcohols (PVAs), high molecular weight poly(ethylene oxide) having a molecular weight greater than about 2000 (up to 10,000,000 Daltons), polyvinylpyrrolidone with a molecular weight of from about 30,000 daltons to about 1,000,000 daltons, a copolymer of N-vinylpyrrolidone and at least one dialkylaminoalkyl (meth)acrylate having 7-20 carbon atoms, and combinations thereof.
  • water soluble cellulose ethers e.g., methyl cellulose (MC), ethyl cellulose, hydroxymethylcellulose, hydroxy
  • Water soluble cellulose ethers and copolymers of vinylpyrrolidone and dimethylaminoethylmethacrylate are most preferred viscosity-enhancing polymers.
  • Copolymers of N-vinylpyrrolidone and dimethylaminoethylmethacrylate are commercially available, e.g., Copolymer 845 and Copolymer 937 from ISP.
  • the viscosity-enhancing polymer is present in the packaging solution in an amount of from about 0.01% to about 5% by weight, preferably from about 0.05% to about 3% by weight, even more preferably from about 0.1% to about 1% by weight, based on the total amount of the packaging solution.
  • a packaging solution can further comprises a polyethylene glycol having a molecular weight of about 1200 or less, more preferably 600 or less, most preferably from about 100 to about 500 daltons.
  • the packaging solution contains a polymeric material having polyethylene glycol segments
  • the packaging solution preferably comprises an ⁇ -oxo-multi-acid or salt thereof in an amount sufficient to have a reduced susceptibility to oxidation degradation of the polyethylene glycol segments.
  • oxo-multi-acid or salt thereof can reduce the susceptibility to oxidative degradation of a PEG-containing polymeric material.
  • Exemplary ⁇ -oxo-multi-acids or biocompatible salts thereof include without limitation citric acid, 2-ketoglutaric acid, or malic acid or biocompatible (preferably ophthalmically compatible) salts thereof. More preferably, an ⁇ -oxo-multi-acid is citric or malic acid or biocompatible (preferably ophthalmically compatible) salts thereof (e.g., sodium, potassium, or the like).
  • the packaging solution can further comprises mucin-like materials, ophthalmically beneficial materials, and/or surfactants.
  • mucin-like materials include without limitation polyglycolic acid, polylactides, and the likes.
  • a mucin-like material can be used as guest materials which can be released continuously and slowly over extended period of time to the ocular surface of the eye for treating dry eye syndrome.
  • the mucin-like material preferably is present in effective amounts.
  • Exemplary ophthalmically beneficial materials include without limitation 2-pyrrolidone-5-carboxylic acid (PCA), amino acids (e.g., taurine, glycine, etc.), alpha hydroxyl acids (e.g., glycolic, lactic, malic, tartaric, mandelic and citric acids and salts thereof, etc.), linoleic and gamma linoleic acids, and vitamins (e.g., B5, A, B6, etc.).
  • PCA 2-pyrrolidone-5-carboxylic acid
  • amino acids e.g., taurine, glycine, etc.
  • alpha hydroxyl acids e.g., glycolic, lactic, malic, tartaric, mandelic and citric acids and salts thereof, etc.
  • linoleic and gamma linoleic acids e.g., B5, A, B6, etc.
  • Surfactants can be virtually any ocularly acceptable surfactant including non-ionic, anionic, and amphoteric surfactants.
  • preferred surfactants include without limitation poloxamers (e.g., Pluronic® F108, F88, F68, F68LF, F127, F87, F77, P85, P75, P104, and P84), poloamines (e.g., Tetronic® 707, 1107 and 1307, polyethylene glycol esters of fatty acids (e.g., Tween® 20, Tween® 80), polyoxyethylene or polyoxypropylene ethers of C 12 -C 18 alkanes (e.g., Brij® 35), polyoxyethyene stearate (Myrj® 52), polyoxyethylene propylene glycol stearate (Atlas® G 2612), and amphoteric surfactants under the trade names Mirataine® and Miranol®.
  • poloxamers e.g., Pluronic
  • the APC coating chemistry in this embodiment imparts a wettable and stable coating to the silicone hydrogel contact lenses.
  • the coating based on acetylene/air mixture e.g., using argon as a carrier gas to generate plasma
  • the coating based on acetylene/air mixture is wettable and stable against the effects of an autoclave.
  • appropriate one or more hydrophilic vinylic monomers e.g., DMA, NVP, HEMA, HEA, and those described below or known to a person skilled in the art
  • the surface properties of the coating are improved, for example, by further improving the substrate surface hydrophilicity and lubricity, etc.
  • hydrophilic vinylic monomers can be used in this aspect of the invention.
  • Suitable hydrophilic vinylic monomers are, without this being an exhaustive list, hydroxyl-substituted C 1 -C 6 alkyl methacrylates or acrylates, hydroxyl-substituted C 1 -C 6 alkyl vinyl ethers, C 1 to C 6 alkyl methacrylamides or acrylamides, di-(C 1 -C 6 alkyl) methacrylamides or acrylamides, N-vinylpyrrole, N-vinyl-2-pyrrolidone, 2-vinyloxazoline, 2-vinyl-4,4'-dialkyloxazolin-5-one, 2- and 4-vinylpyridine, olefinically unsaturated carboxylic acids having a total of 3 to 6 carbon atoms, amino-substituted C 1 -C 6 alkyl- (where the term "amino" also includes quaternary ammonium), mono(C 1
  • hydrophilic vinylic monomers examples include acrylamide, methacrylamide, N,N-dimethylacrylamide (DMA), N,N-dimethylmethacrylamide (DMMA), 2-acrylamidoglycolic acid, 3-acryloylamino-1-propanol, N-hydroxyethyl acrylamide, N- [tris(hydroxymethyl)methyl]-acrylamide, N-methyl-3-methylene-2-pyrrolidone, 1-ethyl-3-methylene-2-pyrrolidone, 1-methyl-5-methylene-2-pyrrolidone, 1-ethyl-5-methylene-2-pyrrolidone, 5-methyl-3-methylene-2-pyrrolidone, 5-ethyl-3-methylene-2-pyrrolidone, 1-n-propyl-3-methylene-2-pyrrolidone, 1-n-propyl-5-methylene-2-pyrrolidone, 1-isopropyl-3-methylene-2-pyrrolidone, 1-isopropyl-3-methylene-2
  • An advantage of this invention relates to the ability to deposit hydrophilic films on polymer substrates so as to achieve enhanced wettability and/or change surface property.
  • a hydrophilic film produced by a plasma polymerisation is thereby obtained (i.e., a hydrophilic film of a plasma-deposed material is deposited on a polymer substrate, especially a silicone hydrogel contact lens).
  • the hydrophilic film produced by plasma polymerisation typically can have a thickness in the range from 1 to 800 nm, preferably of 5 to 500 nm and, more preferably, of 10 to 250 nm.
  • Such a thickness of a hydrophilic film produced by plasma polymerisation can be controlled by the residence time of the substrate in the presence of plasma nozzle jet or by the throughput in the reactor chamber.
  • the thickness of the hydrophilic film can also be increased or decreased by altering the power, time and flow of the plasma jet.
  • a working gas is understood as meaning the composition of a gas or mixture of gases before it is converted into a plasma state.
  • an example working gas can include an inert gas.
  • an example working gas can include both an inert carrier gas and a reagent gas.
  • a working gas is typically produced by volatilizing an organic compound which has been placed in a storage vessel at room temperature and under normal pressure. If the compound is a gas, the gas can be mixed to produce the working gas. If the compound is a liquid, the liquid is volatilized to produce the working gas. A compound can be volatilized by applying a vacuum to, and thermostatically controlling, the storage vessel containing the compound. The storage vessel is typically connected to the plasma reactor by a controllable inlet valve.
  • Exemplary organic compounds and/or gases usable with the system and method of the present invention include aliphatic, alicyclic, araliphatic hydrocarbons or oxahydrocarbons or aromatic compounds, each unsubstituted or substituted by hydroxy, amino, formyl or carboxyl, and containing up to 12 carbon atoms inclusive.
  • Preferred suitable organic compounds and/or gases include alkanes, oxaalkanes, alkenes, oxaalkenes, alkynes, oxaalkynes, mono-, bi- or tricycloalkanes, mono-, bi- or tricyclooxaalkanes or aromatic hydrocarbons, each unsubstituted or substituted by hydroxy, amino, formyl or carboxyl, and containing up to 12 carbon atoms inclusive.
  • suitable organic compounds and/or gases include lower alkanes, lower oxaalkanes, lower alkenes, lower oxaalkenes, lower alkynes, lower oxaalkynes or cycloalkanes, each unsubstituted or substituted by hydroxy, amino, formyl or carboxyl, and containing 3 to 8 carbon atoms, or oxacycloalkanes which are unsubstituted or substituted by hydroxy, amino, formyl or carboxyl and contain 2 to 8 carbon atoms, or unsubstituted benzene or benzene which is substituted by hydroxy, amino, formyl, carboxyl or Ci-Caalkyl.
  • Very particularly preferred organic compounds and/or gases include alkanes, alkynes, alkanols or cycloalkanols, each containing up to 8 carbon atoms inclusive.
  • alkanes alkynes, alkanols or cycloalkanols, each containing up to 8 carbon atoms inclusive.
  • lower qualifying, inter alia, lower alkane, lower alkyne, lower oxaalkane and the like, denotes that the compounds or radicals so defined contain up to 8 carbon atoms inclusive.
  • the substrate to be coated can be a contact lens suitable for extended wear, i.e. for continuous wear of more than six days and six nights up to a time of about 30 days.
  • This type of soft contact lenses includes those comprising polysiloxane and/or perfluoroalkyl-polyether groups which exhibit the desired high oxygen- as well as high ion- and water-permeability.
  • coated contact lenses are obtained which exhibit the following desirable properties as compared to conventionally surface coated contact lenses: increased permeability for oxygen, carbon dioxide, water and ions; excellent wettability, lubricity and stability in the ocular liquid surroundings; improved comfort for the wearer as well as resistance against irreversible deposition of substances occurring in the ocular surroundings, including proteins, lipids, mucins and salts; decreased adhesiveness for microorganisms; decreased tendency of microcrack formation within the coating during sterilization in the autoclave in phosphate buffered saline; and superior on-eye performance including very low cornea swelling, eye irritation and very good mobility on the eye during continuous wear of the lens over an extended time of up to 30 days.
  • a silicone hydrogel contact lens with a coating obtained according to a method of the invention has a wettable surface characterized by having an averaged water contact angle of preferably about 80 degrees or less, more preferably about 65 degrees or less, most preferably about 55 degrees or less.
  • a method of the invention for lens surface treatment does not affect significantly the mechanical and physical properties of a silicone hydrogel contact lens under surface treatment.
  • a silicone hydrogel contact lens with a coating obtained according to a method of the invention has at least one property selected from the group consisting of an oxygen permeability of preferably at least about 40 barrers, more preferably at least about 55 barrers, even more preferably at least about 70 barrers, an elastic modulus of from about 0.1 MPa to about 2.0 MPa, preferably from about 0.2 MPa to about 1.5 MPa, more preferably from about 0.3 MPa to about 1.2 MPa, even more preferably from about 0.4 MPa to about 1.0 MPa, an Ionoflux Diffusion Coefficient, D, of, preferably at least about 1.0 x 10 -5 mm 2 /min, more preferably at least about 2.0 x 10 -5 mm 2 /min, even more preferably at least about 6.0 x 10 -5 mm 2 /min, an equilibrium water content of preferably from about 15% to about 55%
  • the substrate can include contact lens packaging shell manufactured of a polypropylene or other plastic material, whereby the packaging surface is coated to increase the hydrophilicity of the surface and reduce stickiness of a lens that is contained within the package.
  • the wettability of the lenses can also be assessed by determining the time required for the water film to start breaking on the lens surface.
  • lenses are removed from the vial or foil package and washed with distilled (DI) water (e.g. greater than about 100ml) in order to remove loosely bound packaging additives from the lens surface.
  • DI distilled
  • the lens is then placed back in phosphate buffered saline (PBS) for about 5 min and then removed from the PBS and held against a bright light source.
  • PBS phosphate buffered saline
  • Uncoated lenses typically instantly break upon removal from DI water and are assigned a WBUT (i.e., "water break up time” as is typically understood by those having ordinary skill in the art) of 0 seconds. Lenses exhibiting WBUT greater than or equal to about 5 seconds are considered wettable and are expected to exhibit adequate wettability on-eye.
  • WBUT water break up time
  • FIG. 4 An experimental set-up is shown in Figure 4 .
  • a carrier gas 40 is fed thru a plasma generator 42 (e.g., Plasma Treatment System, PT-2000P or PT-2000, from Tri-Star Technologies) that controls the plasma power as well as the flow rate of the carrier gas.
  • Additional gas or gas mixture 44 e.g. air, or oxygen in this example or acetylene in other examples
  • Coating thickness as measured by ellipsometry.
  • the coating parameters are as following: 0.1 LPM of C 2 H 2 , 2 min coating, with helium as the carrier gas. Allow gas flow through the mini chamber for about 5 min before coating.
  • Air sccm
  • Thickness on Si wafer ⁇
  • Contact angel on Si degree 5 839, 783 55, 55 10 946, 869 56, 56 20 773, 792 46, 46 30 664, 641 50, 50 50 308, 380, 406 42, 42 50 411, 390, 374 n/a
  • Example 3 Wettable and Stable Coating with Acetylene (C 2 H 2 )/Air Atmospheric Plasma
  • Uncoated lotrafilcon B lenses from CIBA VISION are coated with the use of PT2000 plasma generator and a mini plasma chamber.
  • An exemplary of parameters used is as following: argon flow rate at 6LPM, 0.1 LPM C 2 H 2 , 40sccm of air, and 20.8KHz frequency for the plasma generator.
  • a total of about 3 minutes of plasma treatment (about 1.5 minutes for each side) is performed using dry lenses (7-15-E). Each lens is “sandwiched” between two metal wire holders. The lenses are flipped after the first 1.5 min plasma treatment. Another experiment is performed using same coating parameters except a total of one time of 3 min plsma treatment (instead of 1.5 min for each side) (7-15-F). Each lens is "sandwiched" between two metal wire holders.
  • Lenses are wettable after once or twice autoclave in PBS, with an average water breakup time of more than 5 seconds after one or twice autoclave.
  • the surface compositions of the lenses are analyzed by x-ray photoelectron spectroscopy (XPS). As compared to uncoated lenses, the C% increases. Uncoated lenses have a c% of 50% or less, The Si% decreases after coating. The uncoated lenses have a Si% of 12% or more.
  • a sub-vacuum coating process can be used to effect the hydrophilic coating on a substrate.
  • the use of such a sub-vacuum coating does not require the use of a carrier gas and/or allows a user to reduce the flow rate.
  • a sub-vacuum of 2 ⁇ 5 torr can be established within the mini chamber when pulled vacuum from a pump for less than about 30sec. Plasma can be generated without using carrier gas.
  • a Tetraethoxysilane (TEOS) bubbler is purchased from Gelest and connected to the atmospheric plasma system.
  • Reusable glass molds similar to the molds shown in Figs. 1-6 in U.S. patent Nos.7,384,590 and 7,387,759 ( Figs. 1-6 ) are coated.
  • the coated glass molds have a contact angle of about 65 degrees, as compared to less than about 10 degrees for uncoated glass molds.
  • the coating on the glass molds is tested for its ability to help to minimize the mode separation force, when using a silicone hydrogel lens formulation that does not contain mold release agent.
  • the mold separation force is very low (in the low 20s as compared to more than 100 for uncoated molds). No star tears are observed for lenses with low mold separation force.
  • the following table is a representation of mold separation forces for 18 lenses made from using two coated glass molds. Group 1 20 21 119 213 25 21 23 22 20 Group 2 23 26 23 20 21 21 22 21 20
  • Example 7 Package Shell Treatment by Atmospheric Plasma
  • Polypropylene (PP) package shells are treated with atmospheric argon plasma and the surface wettability of the treated shells is evaluated by using Acudyne test.
  • the plasma set-up includes a Tri-Star plasma generator (PT-2000P) and a 1 ⁇ 4 inch plastic nozzle. Distance between shell and plasma nozzle is adjusted to 1 mm or 3mm. Plasma intensity tested ranges from 60% to 90% or to 99%.
  • Ar flow rates 30, 40, and 50 SCFH.
  • the wettability of the shell surface increase as indicated by a decrease of surface tension. This is tested by using Accudyne solutions with different surface tension (35, 40, 45, 50 and 60 dyne). The Accudyne solution would spread on a treated surface with similar or lower surface tension and would bead up on a treated surface of higher surface tension. Significant improvement in wettability is obtained when shells are treated, for example, for about 30 seconds at plasma intensity of 90 and Argon flow rate of 30SCFH. No significant difference is observed between argon plasma vs. argon/O 2 plasma.

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  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Mechanical Engineering (AREA)
  • Eyeglasses (AREA)
  • Moulds For Moulding Plastics Or The Like (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)

Claims (12)

  1. Procédé de production de lentilles de contact en hydrogel de silicone prêtes à l'emploi, ayant chacune un revêtement hydrophile de plasma durable, comprenant les étapes qui consistent à:
    (a) générer un flux de plasma atmosphérique à partir d'un gaz de travail par des décharges à pression atmosphérique à une pression atmosphérique environnante, où le gaz de travail comprend au moins un composé organique choisi dans le groupe constitué par un alcane en C1-C12, un oxaalcane ayant jusqu'à 12 atomes de carbone, un alcène en C2-C12, un oxaalcène ayant jusqu'à 12 atomes de carbone, un alcyne en C2-C12, un alcanol en C1-C12, un cycloalcanol ayant jusqu'à 12 atomes de carbone, un oxaalcyne ayant jusqu'à 12 atomes de carbone, un monocyclooxaalcane ayant jusqu'à 12 atomes de carbone, un bicyclooxaalcane ayant jusqu'à 12 atomes de carbone, un tricycloalcane ayant jusqu'à 12 atomes de carbone, un hydrocarbure aromatique ayant jusqu'à 12 atomes de carbone, et leurs combinaisons, où ledit au moins un composé organique est non substitué ou substitué par un groupe hydroxy, amino, formyle ou carboxyle, et contenant jusqu'à 12 atomes de carbone;
    (b) contrôler la continuité du flux de plasma atmosphérique à l'aide d'un générateur électrique;
    (c) introduire le flux de plasma atmosphérique sur une surface d'une lentille de contact en hydrogel de silicone humide ou humide séchée au buvard pour former un revêtement plasma sur la lentille de contact en hydrogel de silicone humide ou humide séchée au buvard;
    (d) placer et sceller la lentille de contact en hydrogel de silicone avec le revêtement plasma dessus dans un emballage pour lentille contenant une solution saline tamponnée; et
    (e) passer à l'autoclave l'emballage pour lentille scellé contenant la lentille de contact en hydrogel de silicone avec le revêtement plasma dessus de manière à obtenir la lentille de contact en hydrogel de silicone prête à l'emploi, où le revêtement plasma sur la lentille de contact en hydrogel de silicone prête à l'emploi subsiste à l'autoclavage et confère à la lentille de contact en hydrogel de silicone prête à l'emploi une hydrophilie/mouillabilité caractérisée par le fait d'avoir un temps de rupture du film d'eau d'au moins environ 5 secondes et/ou pas plus d'environ 30% d'augmentation de l'angle de contact moyen avec l'eau par rapport au même revêtement plasma avant autoclavage.
  2. Procédé selon la revendication 1, dans lequel au moins un composé organique est choisi dans le groupe constitué par un alcane ayant jusqu'à 8 atomes de carbone, un alcyne ayant jusqu'à 8 atomes de carbone, un alcanol ayant jusqu'à 8 atomes de carbone, un cycloalcanol ayant jusqu'à 8 atomes de carbone, et leurs combinaisons.
  3. Procédé selon la revendication 1, dans lequel le composé organique est l'acétylène.
  4. Procédé selon la revendication 1, 2 ou 3, dans lequel le gaz de travail comprend l'air, l'azote, l'oxygène ou un mélange de ceux-ci.
  5. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel le gaz de travail comprend au moins un monomère vinylique choisi dans le groupe constitué par l'acrylamide, le méthacrylamide, le N,N-diméthylacrylamide, N,N-diméthylméthacrylamide, l'acide 2-acrylamidoglycolique, le 3-acryloylamino-1-propanol, le N-hydroxyéthylacrylamide, le N-[tris(hydroxyméthyl)méthyl]acrylamide, la N-méthyl-3-méthylène-2-pyrrolidone, la 1-éthyl-3-méthylène-2-pyrrolidone, la 1-méthyl-5-méthylène-2-pyrrolidone, la 1-éthyl-5-méthylène-2-pyrrolidone, la 5-méthyl-3-méthylène-2-pyrrolidone, la 5-éthyl-3-méthylène-2-pyrrolidone, la 1-n-propyl-3-méthylène-2-pyrrolidone, la 1-n-propyl-5-méthylène-2-pyrrolidone, la 1-isopropyl-3-méthylène-2-pyrrolidone, la 1-isopropyl-5-méthylène-2-pyrrolidone, la 1-n-butyl-3-méthylène-2-pyrrolidone, la 1-tert-butyl-3-méthylène-2-pyrrolidone, le méthacrylate de 2-hydroxyéthyle, l'acrylate de 2-hydroxyéthyle, l'acrylate d'hydroxypropyle, le méthacrylate d'hydroxypropyle, le chlorhydrate de 2-hydroxypropylméthacrylate de triméthylammonium, le chlorhydrate de méthacrylate d'aminopropyle, le méthacrylate de diméthylaminoéthyle, le méthacrylate de glycérol, la N-vinyl-2-pyrrolidone, un alcool allylique, la vinylpyridine, un méthacrylate d'alcoxy(en C1-C4)polyéthylèneglycol ayant un poids moléculaire moyen en poids allant jusqu'à 1500, un acrylate d'alcoxy(en C1-C4)-polyéthylèneglycol ayant un poids moléculaire moyen en poids allant jusqu'à 1500, l'acide méthacrylique, le N-vinylformamide, le N-vinylacétamide, le N-vinylisopropylamide, le N-vinyl-N-méthylacétamide, le N-vinylcaprolactame, et leurs mélanges.
  6. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel le gaz de travail comprend le N,N-diméthylacrylamide, le méthacrylate de 2-hydroxyéthyle, l'acrylate de 2-hydroxyéthyle, la N-vinyl-2-pyrrolidone, le méthacrylate de glycérol, un méthacrylate d'alcoxy(en C1-C4)-polyéthylèneglycol ayant un poids moléculaire moyen en poids allant jusqu'à 1500, un acrylate d'alcoxy(en C1-C4)-polyéthylèneglycol ayant un poids moléculaire moyen en poids allant jusqu'à 1500, l'acide méthacrylique, le N-vinylformamide, le N-vinylacétamide, le N-vinylisopropylamide, le N-vinyl-N-méthylacétamide, l'acrylamide, le méthacrylamide, ou une combinaison de ceux-ci.
  7. Procédé selon l'une quelconque des revendications 1 à 6, dans lequel le gaz de travail comprend un gaz vecteur comprenant au moins un gaz inerte choisi dans le groupe constitué par l'argon, l'hélium, le xénon, et leurs combinaisons.
  8. Procédé selon l'une quelconque des revendications 1 à 7, dans lequel le flux de plasma atmosphérique est introduit sur la surface de la lentille de contact en hydrogel de silicone humide ou humide séchée au buvard par l'intermédiaire d'une buse à pression atmosphérique.
  9. Procédé selon l'une quelconque des revendications 1 à 7, dans lequel, dans l'étape (c), un nuage de plasma uniforme entoure complètement ou se répand sur la couche limite d'une surface de substrat.
  10. Procédé selon l'une quelconque des revendications 1 à 7, dans lequel l'étape (c) est réalisée dans une chambre comportant une vanne d'entrée pour introduire le flux de plasma dans la chambre et une vanne de sortie pour libérer le flux de plasma provenant de la chambre à un débit défini.
  11. Procédé selon l'une quelconque des revendications 1 à 10, comprenant en outre le contrôle du flux de plasma atmosphérique à l'aide d'un amplificateur de puissance, dans lequel l'amplificateur de puissance est adapté pour produire un flux qui est continu ou pulsé.
  12. Procédé selon l'une quelconque des revendications 1 à 11, dans lequel la lentille de contact en hydrogel de silicone prête à l'emploi possède au moins une propriété choisie dans le groupe constitué par: (i) un angle de contact moyen avec l'eau d'environ 80 degrés ou moins, plus préférablement, d'environ 65 degrés ou moins, le plus préférablement, d'environ 55 degrés ou moins; (ii) une perméabilité à l'oxygène qui est, de préférence, d'au moins environ 40 barrers, plus préférablement, d'au moins environ 55 barrers, encore plus préférablement, d'au moins environ 70 barrers; (iii) un module élastique d'environ 0,1 MPa à environ 2,0 MPa, de préférence, d'environ 0,2 MPa à environ 1,5 MPa, plus préférablement, d'environ 0,3 MPa à environ 1,2 MPa, encore plus préférablement, d'environ 0,4 MPa à environ 1,0 MPa; (iv) un "Ionoflux Diffusion Coefficient" D qui est, de préférence, d'au moins environ 1,0 x 10-5 mm2/min, plus préférablement, d'au moins environ 2,0 x 10-5 mm2/min, encore plus préférablement, d'au moins environ 6,0 x 10-5 mm2/min; (v) une teneur en eau à l'équilibre qui est, de préférence, d'environ 15% à environ 55%, plus préférablement, d'environ 20% à environ 38% en poids lorsqu'elle est complètement hydratée; et (vi) leurs combinaisons.
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US9067372B2 (en) 2015-06-30
CN103249544A (zh) 2013-08-14
CN103249544B (zh) 2016-02-03
EP2646228A1 (fr) 2013-10-09
US20120137635A1 (en) 2012-06-07
CN103237651B (zh) 2016-02-10
CN103237651A (zh) 2013-08-07
EP2646229A1 (fr) 2013-10-09
EP2646228B1 (fr) 2014-09-17
US9156213B2 (en) 2015-10-13
WO2012074859A1 (fr) 2012-06-07
US20120139137A1 (en) 2012-06-07
MY157325A (en) 2016-05-31
SG190057A1 (en) 2013-06-28
MY161676A (en) 2017-05-15
SG190061A1 (en) 2013-06-28
WO2012074861A1 (fr) 2012-06-07

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